Genome assembly and annotation of Acropora pulchra from Mo'orea French Polynesia.

GigaByte (Hong Kong, China) Pub Date : 2025-04-10 eCollection Date: 2025-01-01 DOI:10.46471/gigabyte.153
Trinity Conn, Jill Ashey, Ross Cunning, Hollie M Putnam
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引用次数: 0

Abstract

Reef-building corals are integral ecosystem engineers of tropical reefs but face threats from climate change. Investigating genetic, epigenetic, and environmental factors influencing their adaptation is critical. Genomic resources are essential for understanding coral biology and guiding conservation efforts. However, genomes of the coral genus Acropora are limited to highly-studied species. Here, we present the assembly and annotation of the genome and DNA methylome of Acropora pulchra from Mo'orea, French Polynesia. Using long-read PacBio HiFi and Illumina RNASeq, we generated the most complete Acropora genome to date (BUSCO completeness of 96.7% metazoan genes). The assembly size is 518 Mbp, with 174 scaffolds, and a scaffold N50 of 17 Mbp. We predicted 40,518 protein-coding genes and 16.74% of the genome in repeats. DNA methylation in the CpG context is 14.6%. This assembly of the A. pulchra genome and DNA methylome will support studies of coastal corals in French Polynesia, aiding conservation and comparative studies of Acropora and cnidarians.

法属波利尼西亚莫奥利亚地区鹿角蕨基因组组装与注释。
造礁珊瑚是热带珊瑚礁不可或缺的生态系统工程师,但也面临着气候变化的威胁。研究影响它们适应的遗传、表观遗传和环境因素至关重要。基因组资源对于了解珊瑚生物学和指导保护工作至关重要。然而,珊瑚属Acropora的基因组仅限于高度研究的物种。本文报道了法属波利尼西亚莫奥利亚(Mo’orea)鹿角蕨(Acropora pulchra)基因组和DNA甲基化组的组装和注释。使用长读PacBio HiFi和Illumina RNASeq,我们生成了迄今为止最完整的Acropora基因组(96.7%的后生动物基因的BUSCO完整性)。装配尺寸为518 Mbp,包含174个支架,其中一个支架N50为17 Mbp。我们预测了40,518个蛋白质编码基因和16.74%的基因组重复序列。CpG背景下的DNA甲基化率为14.6%。A. pulchra基因组和DNA甲基组的组装将支持法属波利尼西亚沿海珊瑚的研究,有助于Acropora和刺胞动物的保护和比较研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.60
自引率
0.00%
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0
审稿时长
5 weeks
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